Team, Visitors, External Collaborators
Overall Objectives
Research Program
Application Domains
Highlights of the Year
New Software and Platforms
New Results
Bilateral Contracts and Grants with Industry
Partnerships and Cooperations
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Section: Research Program

Regulation and signaling: detecting complex and discriminant signatures of phenotypes

On the contrary to metabolic networks, regulatory and signaling processes in biological systems involves agents interacting at different granularity levels (from genes, non-coding RNAs to protein complexes) and different time-scales. Our focus is on the reconstruction of large-scale networks involving multiple scales processes, from which controllers can be extracted with symbolic dynamical systems methods. A particular attention is paid to the characterization of products of genes (such as isoform) and of perturbations to identify discriminant signature of pathologies.

Research topics

Genomic level: characterizing gene structure with grammatical languages and conservation information The subject here is to accurately represent gene structure, including intron/exon structure, for predicting the products of genes, such as isoform transcripts, and comparing the expression potential of a eukaryotic gene according to its context (e.g. tissue) or according to the species. Our approach consists in designing grammatical and comparative-genomics based models for gene structures able to detect heterogeneous functional sites (splicing sites, regulatory binding sites...), functional regions (exons, promotors...) and global constraints (translation into proteins) [46]. Accurate gene models are defined by identifying general constraints shaping gene families and their structures conserved over evolution. Syntactic elements controlling gene expression (transcription factor binding sites controlling transcription; enhancers and silencers controlling splicing events...), i.e. short, degenerated and overlapping functional sequences, are modeled by relying on the high capability of SVG grammars to deal with structure and ambiguity [66].

System level: extracting causal signatures of complex phenotypes with systems biology frameworks The main challenge we address is to set up a generic formalism to model inter-layer interactions in large-scale biological networks. To that goal, we have developed several types of abstractions: multi-experiments framework to learn and control signaling networks [11], multi-layer reactions in interaction graphs [47], and multi-layer information in large-scale Petri nets [43]. Our main issues are to scale these approaches to standardized large-scale repositories by relying on the interoperable Linked Open Data (LOD) resources and to enrich them with ad-hoc regulations extracted from sequence-based analysis. This will allow us to characterize changes in system attractors induced by mutations and how they may be included in pathology signatures.

Associated software tools

Logol software is designed for complex pattern modelling and matching [url]. It is a swiss-army-knife for pattern matching on DNA/RNA/Protein sequences, based on expressive patterns which consist in a complex combination of motifs (such as degenerated strings) and structures (such as imperfect stem-loop ou repeats) [2]. Logol key features are the possibilities (i) to divide a pattern description into several sub-patterns, (ii) to model long range dependencies, and (iii) to enable the use of ambiguous models or to permit the inclusion of negative conditions in a pattern definition. Therefore, Logol encompasses most of the features of specialized tools (Vmatch, Patmatch, Cutadapt, HMM) and enables interplays between several classes of patterns (motifs and structures), including stem-loop identification in CRISPR.

Caspo software Cell ASP Optimizer (Caspo) constitutes a pipeline for automated reasoning on logical signaling networks (learning, classifying, designing experimental perturbations, identifying controllers, take time-series into account) [url]. The software handles inherent experimental noise by enumerating all different logical networks which are compatible with a set of experimental observations [11]. The main advantage is that it enables a complete study of logical network without requiring any linear constraint programs.

Cadbiom package aims at building and analyzing the asynchronous dynamics of enriched logical networks [url] It is based on Guarded transition semantic and allows synchronization events to be investigated in large-scale biological networks [43]. For instance, it was designed to allow controler of phenotypes in large-scale knowledge databases (PID) to be curated and analyzed [5].